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Nucleophilic imidoesterification of dicarbonyl compounds with cyanatobenzenes through C-C bond formation |
Hang Maa, Yang Hea, Ruo-Feng Huanga, Xiao-Hui Zhanga, Jing Pana, Jia-Qiang Lia, Chao Hea, Xue-Ge Linga, Xuan-Lun Wangc, Yan Xionga,b |
a School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China;
b Chongqing Key Laboratory of Chemical Process for Clean Energy and Resource Utilization, Chongqing University, Chongqing 400044, China;
c College of Materials Science and Engineering, Chongqing University of Technology, Chongqing 400054, China |
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Abstract Under neat conditions, an efficient method for synthesis of imidoesters has been developed using cyanatobenzenes and dicarbonyl compounds. Nucleophilic addition spontaneously occurred between the two kinds of materials at room temperature with yields of up to 90%. A mechanism directed towards to the imidoester formation has been proposed.
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Received: 22 May 2014
Published: 13 June 2014
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Fund: We gratefully acknowledge for funding from the SRTP of Chongqing University for undergraduate cultivation (H. Ma and Y. He), the National Natural Science Foundation of China (Nos. 21372265 and 61271059), the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry, the Natural Science Foundation Project of CQ CSTC (Nos. CSTC2013jcyjA0217 and CSTC2010BB4086), and the Fundamental Research Funds for the Central Universities (Nos. CQDXWL-2013-Z012 and CDJZR-14225502). |
Corresponding Authors:
Yan Xiong
E-mail: xiong@cqu.edu.cn
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